Clinical Trials Manager

🔥 0 minutes ago

🏄 California, New Jersey, +2 more states – Remote

🏄 California – Remote 🏖️ New Jersey – Remote 🌲 North Carolina – Remote ☕ Washington – Remote

💵 $133.2k - $172.4k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

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Gilead Sciences

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Gilead Sciences is a leading biopharmaceutical company that focuses on discovering, developing, and delivering innovative therapeutics for patients with life-threatening diseases. The company is highly recognized for its contributions in virology, particularly HIV and hepatitis, and is actively expanding its therapeutic reach into fields like oncology and inflammation. Gilead has a strong pipeline of medicines, with over 25 products available globally and 50 clinical programs. Known for its commitment to health equity, the company also actively funds HIV research and causes. Gilead's dedication to scientific innovation and health equity aims to tackle the world's most pressing health challenges, improving patient lives globally.

📋 Description

• Coordinating and supervising all aspects of a clinical study • Monitoring clinical trial sites • Assisting Clinical Program Manager in overall study management • Drafting and coordinating review of relevant documents including protocols, informed consents, case report forms, monitoring plans • Maintaining study timelines • Contributing to development of study budget • Managing CROs/vendors • Ensuring effectiveness of site budget/contract process • Training CROs, vendors, investigators, and study coordinators on study requirements • Design scientific communications within the company

🎯 Requirements

• BS or BA in a relevant scientific discipline and 6+ years of relevant experience OR RN license (2 or 3 year certificate) and 6+ years of relevant experience • Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials • Ability to prioritize multiple tasks • Ability to communicate and explain protocol requirements to others • Experience in therapy areas like Hematology, Oncology, Rheumatology, or Autoimmune disorders is helpful.

🏖️ Benefits

• Discretionary annual bonus • Discretionary stock-based long-term incentives (eligibility may vary based on role) • Paid time off • Medical, dental, vision, and life insurance plans